solute carrier family 52, riboflavin transporter, member 2 isoform X2 - Protein

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Impact of natural mutations on the riboflavin transporter 2 and their relevance to human riboflavin transporter deficiency 2. [IUBMB Life. 2022]
Impact of natural mutations on the riboflavin transporter 2 and their relevance to human riboflavin transporter deficiency 2.
Console L, Tolomeo M, Cosco J, Massey K, Barile M, Indiveri C. IUBMB Life. 2022 Jul; 74(7):618-628. Epub 2021 Aug 24.
Functional Study of the Human Riboflavin Transporter 2 Using Proteoliposomes System. [Methods Mol Biol. 2021]
Functional Study of the Human Riboflavin Transporter 2 Using Proteoliposomes System.
Console L, Tolomeo M, Indiveri C. Methods Mol Biol. 2021; 2280:45-54.
Mitochondrial and Peroxisomal Alterations Contribute to Energy Dysmetabolism in Riboflavin Transporter Deficiency. [Oxid Med Cell Longev. 2020]
Mitochondrial and Peroxisomal Alterations Contribute to Energy Dysmetabolism in Riboflavin Transporter Deficiency.
Colasuonno F, Niceforo A, Marioli C, Fracassi A, Stregapede F, Massey K, Tartaglia M, Bertini E, Compagnucci C, Moreno S. Oxid Med Cell Longev. 2020; 2020:6821247. Epub 2020 Aug 12.

RefSeq genomic sequence
See the genomic reference sequence for the SLC52A2 gene (NG_032872.2).
RefSeq mRNA
See reference mRNA sequence for the SLC52A2 gene (XM_017013821.2).

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GlyGen glycoinformatics resource [GlyGen glycoinformatics resou...]
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reagents [ExactAntigen/Labome]
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